Hydrochloric Acid → Methyl 3-bromo-4-hydroxy-5-(3-morpholino-3-oxopropanoyl)benzoate

HRID 41178

Reaktionsgleichung

Reaktionsgleichung von HRID 41178
C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[C:11]([C:14]1[CH:15]=[C:16]([CH:21]=[C:22]([Br:25])[C:23]=1[OH:24])[C:17]([O:19][CH3:20])=[O:18])(=[O:13])[CH3:12].[N:26]1([C:32](Cl)=[O:33])[CH2:31][CH2:30][O:29][CH2:28][CH2:27]1.Cl>C1COCC1.O.C(Cl)Cl>[Br:25][C:22]1[CH:21]=[C:16]([CH:15]=[C:14]([C:11](=[O:13])[CH2:12][C:32]([N:26]2[CH2:31][CH2:30][O:29][CH2:28][CH2:27]2)=[O:33])[C:23]=1[OH:24])[C:17]([O:19][CH3:20])=[O:18]

Komponenten

8

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of lithium bis(trimethylsilyl)amide (1.41 L, 1406 mmol) at −65° C. under nitrogen was added dropwise methyl 3-acetyl-5-bromo-4-hydroxybenzoate (120 g, 439 mmol) in THF (1.2 L). The solution was allowed to warm to 0° C., and maintained at this temperature for 1 h. The solution was cooled back to −65° C. and morpholine-4-carbonyl chloride (0.055 L, 483 mmol) was added. The mixture was stirred at room temperature for 2 h then cooled to −30° C., DCM (1.5 L) and water (1 L) were added followed by dropwise addition of HCl 6N (500 mL) then HCl 2N (300 mL) until pH 7, the aqueous solution was extracted with DCM (3×). The combined extracts were dried over MgSO4 and evaporated. The crude product was triturated in MTBE to obtain methyl 3-bromo-4-hydroxy-5-(3-morpholino-3-oxopropanoyl)benzoate (153 g, 90%) as a beige solid. Mass Spectrum: m/z [M+H]+=388.

Aufarbeitung

  1. temperaturemaintained at this temperature for 1 h
  2. temperatureThe solution was cooled back to −65° C.
  3. temperaturethen cooled to −30° C.
  4. extractionHCl 2N (300 mL) until pH 7, the aqueous solution was extracted with DCM (3×)
  5. dry with materialThe combined extracts were dried over MgSO4
  6. customevaporated
  7. customThe crude product was triturated in MTBE

Quellen und Nachweise

ORD-Eintrag
ord-ac98ea7eac74444ebae29bd7fb48f7ea
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08530470B2

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